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Synthesis, Characterization and Biological Evaluation of Metal(II) Complexes Containing Triphenylphosphine and Schiff Base Ligand Based on 3-Methoxysalicylaldehyde
Corresponding Author(s) : C. Umarani
Asian Journal of Chemistry,
Vol. 33 No. 8 (2021): Vol 33 Issue 8, 2021
Abstract
Schiff base ligand (HL) derived from condensation of 3-methoxy salicylaldehyde with 4-aminobenzoic acid and its metal(II) complexes containing triphenylphosphine of the type [MCl(PPh3)(L)] (M = Ni2+, Co2+ or Cu2+; L = bitendate Schiff base ligand) have been synthesized. All the metal(II) complexes were characterized by analytical and spectroscopic (FT-IR, electronic, ESI-Mass, ESR, 1H, 13C NMR and 31P NMR) techniques. All the synthesized compounds were evaluated for in vitro antimicrobial efficiency against Gram-positive bacteria, Gram-negative bacteria and fungai using the agar well diffusion method. Anticancer activity in vitro of the ligand and its metal(II) complexes were also screened against MCF-7 cancer cell lines (human breast cancer cell line).
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References
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M. Sonmez, H.G. Sogukomerogullari, F. Oztemel and I. Berber, Med. Chem. Res., 23, 3451 (2014); https://doi.org/10.1007/s00044-014-0925-0
D. Chaturvedi and M. Kamboj, Chem. Sci. J., 7, 1 (2016); https://doi.org/10.4172/2150-3494.1000e114
B. Iftikhar, K. Javed, M.S.U. Khan, Z. Akhter, B. Mirza and V. Mckee, J. Mol. Struct., 1155, 337 (2018); https://doi.org/10.1016/j.molstruc.2017.11.022
M.S. Alam, J.H. Choi and D.U. Lee, Bioorg. Med. Chem., 20, 4103 (2012); https://doi.org/10.1016/j.bmc.2012.04.058
S.B. Desai, P.B. Desai and K.R. Desai, Heterocycl. Commun., 7, 83 (2001); https://doi.org/10.1515/HC.2001.7.1.83
S. Sarkar, S.K. Nag, A.P. Chattopadhyay, K. Dey, S.M. Islam, A. Sarkar and S. Sarkar, J. Mol. Struct., 1160, 9 (2018); https://doi.org/10.1016/j.molstruc.2018.01.035
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R.N. Egekenze, Y. Gultneh and R. Butcher, Inorg. Chim. Acta, 478, 232 (2018); https://doi.org/10.1016/j.ica.2018.01.027
A. Hasaninejad, S. Mojikhalifeh and M. Beyrati, Appl. Organomet. Chem., 32, e4380 (2018); https://doi.org/10.1002/aoc.4380
G.L. Backes, D.M. Neumann and B.S. Jursic, Bioorg. Med. Chem., 22, 4629 (2014); https://doi.org/10.1016/j.bmc.2014.07.022
E. Pelttari, M. Lehtinen and H. Elo, Z. Naturforsch. C, 66, 571 (2011); https://doi.org/10.1515/znc-2011-11-1206
L.A. Saghatforoush, A. Aminkhani and F. Chalabian, Transition Met. Chem., 34, 899 (2009); https://doi.org/10.1007/s11243-009-9279-8
M.S. Refat, I.M. El-Deen, Z.M. Anwer and S. El-Ghol, J. Coord. Chem., 62, 1709 (2009); https://doi.org/10.1080/00958970802684205
C.D. Sheela, C. Anitha, P. Tharmaraj and D. Kodimunthri, J. Coord. Chem., 63, 884 (2010); https://doi.org/10.1080/00958971003660416
M. Gielen and E.R.T. Tiekink, Metalotherapeutic Drugs and MetalBased Diagnostic Agents: The Uses of Metal in Medicine, John Wiley & Sons: New York (2005).
A. Ray, G.M. Rosair, R. Kadam and S. Mitra, Polyhedron, 28, 796 (2009); https://doi.org/10.1016/j.poly.2008.12.040
J. Vanco, J. Marek, Z. Travnicek, E. Racanska, J. Muselik and O. Svajlenova, J. Inorg. Biochem., 102, 595 (2008); https://doi.org/10.1016/j.jinorgbio.2007.10.003
M.M. Tamizh, K. Mereiter, K. Kirchner and R. Karvembu, J. Organomet. Chem., 700, 194 (2012); https://doi.org/10.1016/j.jorganchem.2011.12.016
R. Prabhakaran, S.V. Renukadevi, R. Karvembu, R. Huang, J. Mautz, G. Huttner, R. Subashkumar and K. Natarajan, Eur. J. Med. Chem., 43, 268 (2008); https://doi.org/10.1016/j.ejmech.2007.03.006
G. Erre, S. Enthaler, K. Junge, S. Gladiali and M. Beller, Coord. Chem. Rev., 252, 471 (2008); https://doi.org/10.1016/j.ccr.2007.09.021
A.I. Vogal, Textbook of Practical Organic Chemistry, Eds.: 5, ELBS: London (1989).
L.M. Venanzi, J. Chem. Soc., 719 (1958); https://doi.org/10.1039/jr9580000719
M. Balouiri, M. Sadiki and S.K. Ibnsouda, J. Pharm. Anal., 6, 71 (2016); https://doi.org/10.1016/j.jpha.2015.11.005
J.D. Burton, Methods Mol. Med., 110, 69 (2005);
M.M. Tamizh, B. Varghese, A. Endo and R. Karvembu, Spectrochim. Acta A Mol. Biomol. Spectrosc., 77, 411 (2010); https://doi.org/10.1016/j.saa.2010.06.004
M.M. Tamizh, K. Mereiter, K. Kirchner, B.R. Bhat and R. Karvembu, Polyhedron, 28, 2157 (2009); https://doi.org/10.1016/j.poly.2009.04.021
M.B. Ferrari, S. Capacchi, F. Bisceglie, G. Pelosi and P. Tarasconi, Inorg. Chim. Acta, 312, 81 (2001); https://doi.org/10.1016/S0020-1693(00)00339-X
N.C. Kasuga, K. Sekino, C. Koumo, N. Shimada, M. Ishikawa and K. Nomiya, J. Inorg. Biochem., 84, 55 (2001); https://doi.org/10.1016/S0162-0134(00)00221-X
S. Güveli, N. Özdemir, T. Bal-Demirci, B. Ülküseven, M. Dinçer and Ö. Andaç, Polyhedron, 29, 2393 (2010); https://doi.org/10.1016/j.poly.2010.05.004
S. Chandra and U. Kumar, Spectrochim. Acta A Mol. Biomol. Spectrosc., 61, 219 (2005); https://doi.org/10.1016/j.saa.2004.03.036.
B.G. Tweedy, Phytopathology, 55, 910 (1964).